Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,496 recalls have been distributed to District of Columbia in the last 12 months.
Showing 18201–18220 of 27,451 recalls
Recalled Item: Biograph mCT S(40)-4R Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mCT S(64)-4R Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mCT S(64)-3R Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mCT X-3R Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH mCT 20 Excel Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mCT Flow 40-4R Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware, through our...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AxIEM Touch N Go Pointer Probe. Model Number: 9735318. Placed Recalled by...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the AxIEM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: URF-P6 Uretero-reno fiberscope and URF-P6R Uretero-reno fiberscope Recalled...
The Issue: Olympus is recalling the URF-P6/P6R endoscopes due to a similar device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uretero-reno videoscope URF-V2 and URF-V2R endoscope and accessories The...
The Issue: Olympus has received complaints regarding the breakage of the endoscope's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rigid Laryngostroboscopes The Rigid Laryngostroboscopes Recalled by Pentax...
The Issue: Pentax is initiating a Field Correction to revise the Instructions for Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Great Basin Staph lD/R Blood Culture Panel The Great Basin Recalled by Great...
The Issue: The Great Basin Staph ID/R Panel is being recalled because the S. aureus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline E-Z Lubricating Jelly Recalled by MEDLINE IND Due to Product was not...
The Issue: Product was not sterilized. Product was shipped to distribution centers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Velara Generator with an old Firmware version used with the Recalled by...
The Issue: System may lock up.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Eye Station. f/k/a: DFC-1024 & DFC-512 Digital Imaging System Recalled...
The Issue: Merge received reports of Merge Eye Station being unable to capture images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatLock¿ CV Plus w/Pigtail. Product Code: CV0220CE & CV0220. Packaged...
The Issue: Bard Access Systems announces a voluntary field action for the StatLock¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Velara Generator with an old Firmware version used with Philips Recalled by...
The Issue: System may lock up.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatLock¿ PICC Plus Crescent Foam. Product Code: VPPCSP & VPPCSPCE. Recalled...
The Issue: Bard Access Systems announces a voluntary field action for the StatLock¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amplia MRI" CRT -D SureScan" Recalled by Medtronic Inc., Cardiac Rhythm and...
The Issue: During internal testing conducted as part of next generation product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tiger Screw Sterilization Tray Base Assembly Model 210-00-001 Revision N...
The Issue: Four lots of Tiger Screw Sterilization Tray Base Assemblies were released to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q/Q.zen Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens initiated a corrective action to address two possible, mutually...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.